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Lunds & Byerly's Curry Powder Sweet bottles were filled with sesame seeds but labeled as curry powder. This mislabeling creates a risk for people with sesame allergies who may consume the product expecting curry powder. The affected lot code is 0082026U00232 with a best-by date of 01/26/2029.

Moderate·FDA·Jun 10, 2026

Second Nature Keto Crunch Smart Mix 10-ounce pouches may contain undeclared cashews, pistachios, and dried cherries. These allergens are not listed on the label, which is a serious concern for people with tree nut allergies. The product was distributed nationwide through retail stores and online.

Moderate·FDA·Jun 10, 2026

Market of Choice Vegan Kale Caesar Salad contains sesame seeds in the Za'atar spice mixture, but sesame is not listed on the label. People with sesame allergies could have a serious reaction if they eat this product.

Moderate·FDA·Jun 10, 2026

Jesse's Bakery is recalling two coleslaw products, My Wife's Slaw and My Wife's Slaw Jalapeno Heat, sold in 8 oz. and 16 oz. glass mason jars. The products were made and distributed without an approved food establishment inspection, and the required safety parameters could not be verified. They were sold in Alabama, Ohio, Texas, and West Virginia, and no injuries have been reported.

Moderate·FDA·Jun 10, 2026·My Wife's Slaw2 products

Creative Compounds, LLC is recalling Betaine Anhydrous (Lot SWT2025100101, expiration September 2027) because it may contain small pieces of carbon steel (1–2mm). The affected material was distributed to five accounts in Florida, New Jersey, Texas, Georgia, and Oregon.

Moderate·FDA·Jun 10, 2026·Creative Compounds

Straus Family Creamery is recalling five flavors of its organic super premium ice cream, sold in pint and quart containers, because they may contain small metal pieces. The products were distributed in 17 states, including CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA and WI. No injuries have been reported.

Moderate·FDA·Jun 10, 2026·Straus Family Creamery5 products

The Brownie Baker Inc. is recalling café Nouria blueberry muffins (6 oz, UPC 811070033986, Lot 6082) because they contain walnuts that are not declared on the label. People with walnut allergies or sensitivities could have a serious reaction if they eat these muffins without knowing walnuts are inside.

Moderate·FDA·Jun 10, 2026

The CNG tank support bracket in certain Cummins Clean Fuel Technologies 75DGE fuel systems can become deformed during a side-impact crash, potentially causing the tank to dislodge or detach. A loose tank can leak fuel, creating a fire risk.

Moderate·NHTSA·Jun 9, 2026·Natural Gas Fuel Systems, LLC dba CCFT

GO Raw LLC is expanding a recall of freeze-dried chicken pet food due to potentially low levels of thiamine (vitamin B1). Cats and dogs eating this food over time may develop deficiency symptoms ranging from decreased appetite and vomiting to neurological problems like neck bending, poor coordination, and seizures.

Moderate·FDA·Jun 8, 2026·GO Raw

Pearl Milling Company Original Pancake & Waffles mix (5.99 oz pouches) sold in Puerto Rico contains milk and soy but was labeled as "may contain" instead of "contains." People with milk or soy allergies could have a serious allergic reaction if they consume it.

Moderate·FDA·Jun 4, 2026

Tiny Land children's play tents contain fiberglass poles that can shed fibers, causing skin and eye irritation. The company has received eight reports of fiber shedding resulting in irritation. The tents were sold online from November 2025 through March 2026.

Moderate·CPSC·Jun 4, 2026·Tiny Land

Some Medline EYE TRAY-LF convenience kits (SKU DYNJ21627P) contain syringes labeled as tuberculin syringes on the box, but the actual syringes inside are insulin syringes. Using the wrong syringe type could lead to incorrect dosing.

Moderate·FDA·Jun 3, 2026

Philips is recalling Azurion and Allura imaging systems because the hard drives in their PCs may slow down as they age, especially after six years of use. Depending on the system, this can cause loss of imaging function, and in Allura systems it may also cause loss of motorized movement or data loss. A system restart may temporarily restore function. No injuries have been reported, and the recall covers 2 product lines with about 3,069 affected units.

Moderate·FDA·Jun 3, 20262 products

GE HealthCare has identified a situation where the ApexPro CARESCAPE Telemetry Server (versions 5.0 and 6.0) can lose ECG and SpO2 monitoring data if the system loses network connection to the central monitoring station. This affects 14 units used in hospitals and clinical settings.

Moderate·FDA·Jun 3, 20266 products

A limited number of Medtronic 1x4 Pocket Adaptor Kits (Models 64001 and 64002) used in deep brain stimulation devices are labeled with incorrect Use-By-Dates. The mislabeled kits may no longer be safe or effective for their intended use.

Moderate·FDA·Jun 3, 20262 products

Devicor Medical Products is recalling HydroMARK Breast Biopsy Site Marker Model 4010-02-15-T3 due to incorrect labeling on individual packages inside boxes. Some boxes labeled as T3 markers may contain packages labeled as T4 markers, which could lead to use of the wrong marker type during a breast biopsy procedure.

Moderate·FDA·Jun 3, 2026·Devicor

Halyard Purezero Ultraviolet Nitrile Exam Gloves in sizes XS through XL failed to meet chemical permeation performance standards, meaning they may not provide adequate protection against certain chemicals. This affects approximately 452,500 units distributed nationwide.

Moderate·FDA·Jun 3, 2026·Halyard

Fly By Jing Creamy Sesame Noodles (3.8 oz packets) may contain peanuts due to cross-contamination during production, even though peanuts are not listed on the label. This poses a serious risk to people with peanut allergies. The recall affects approximately 3,419 cases with best-by dates between October 15, 2026 and March 23, 2027.

Moderate·FDA·Jun 3, 2026

AbbVie is recalling specific lots of PRED MILD (prednisolone acetate) eye drops because they failed stability testing. The affected product may not maintain its intended strength or safety over time. Two lots are involved, with an expiration date of August 2026.

Moderate·FDA·Jun 3, 2026·AbbVie

AVEVA nicotine patches (14 mg) distributed by Rugby Laboratories have elevated levels of chemical impurities that exceed safety standards for shelf life. The issue was discovered during stability testing of specific lots. No injuries have been reported.

Moderate·FDA·Jun 3, 2026·AVEVA

D'Dioses fruit popsicles in 3.7 oz. packages may contain undeclared milk, pecans, pistachios, Yellow #5, and Red #40. The recall affects products made before April 27, 2026, in multiple flavors distributed in New Jersey, New York, Pennsylvania, and Connecticut. People with allergies or sensitivities to these ingredients could have serious reactions.

Moderate·FDA·May 27, 2026

SkinnyDipped Dark Chocolate Coconut Almond Bites in certain lots may contain undeclared peanut or peanut butter, even though peanuts are not an intended ingredient. The issue was discovered after a consumer found peanut butter–containing products in the wrapper. People with peanut allergies could have a serious allergic reaction.

Moderate·FDA·May 27, 2026

Philips is recalling X-ray tube cooling units, type CU3101, that were made between February 2016 and May 2020. The deaeration hose may degrade and leak oil, which can reduce cooling. When oil flow drops too low, the system switches to low-dose fluoroscopy and shows a tube cooler message that restarting does not clear. The recall covers 3 product lines with about 5,000 affected units, and no injuries have been reported.

Moderate·FDA·May 27, 20263 products

C.R. Bard has recalled certain Silastic Brand Foley Catheters (5cc and 30cc models) due to staining on the catheter surface. The affected catheters were distributed across the U.S. and Canada.

Moderate·FDA·May 27, 2026

Certain Philips Azurion fluoroscopy systems may experience mechanical wear in the Float Tabletop control, which could impair the longitudinal and transverse (side-to-side and front-to-back) movement of the examination table. This wear could affect the system's ability to position patients correctly during imaging procedures.

Moderate·FDA·May 27, 2026

Medtronic is recalling nine models of retrograde cannulas used in cardiopulmonary bypass procedures. Certain lots may have a sterile barrier that could be breached, which could compromise the product's sterility. No injuries have been reported.

Moderate·FDA·May 27, 20269 products

The straight inserter tool on certain OneLIF Interbody Cage implants may fail to attach properly to the cage. This could prevent secure engagement during spinal fusion surgery, potentially causing procedural delays or requiring surgeons to choose a different implant.

Moderate·FDA·May 27, 2026·Novapproach Spine

ICU Medical oncology infusion kits with extension sets may develop leaks during chemotherapy administration. If a leak occurs during therapy, patients may receive less medication than intended, and healthcare workers or patients could be exposed to hazardous drugs.

Moderate·FDA·May 27, 2026

Tangent Endoscopy's Single Use Digital Catheter (models TNG4002-IND and TNG-4007-6pk) can develop fractures at the tip of the shaft during use. While the fractured pieces have not completely detached in reported cases, a broken catheter tip could affect device function or potentially cause patient harm.

Moderate·FDA·May 27, 2026·Tangent Endoscopy

Becton Dickinson is recalling 3 Swan-Ganz catheter product lines, with 589,459 affected units in total. The blue proximal injectate lumen hub can leak or break because of manufacturing and material changes, which may lead to infection, medication loss, or blood loss. No injuries have been reported, and the products were distributed across the US and in many other countries.

Moderate·FDA·May 27, 20263 products